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Politano

Showing results (371-380 of 638) with videos related to

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The Journal of Molecular Diagnostics : JMD|December 5, 2009
One hundred twenty-one dystrophin point mutations detected from stored DNA samples by combinatorial denaturing high-performance liquid chromatographyAnnalaura Torella, Amelia Trimarco, Francesca Del Vecchio Blanco, et al.
Brain & Development|November 29, 2022
A novel variant in NEUROD2 in a patient with Rett-like phenotype points to Glu130 codon as a mutational hotspotDavide Politano, Simone Gana, Elena Pezzotti, et al.
Journal of Cardiovascular Electrophysiology|October 4, 2019
SERUM cardiac-specific biomarkers and atrial fibrillation in myotonic dystrophy type IVincenzo Russo, Anna Rago, Luigi Atripaldi, et al.
Neuromuscular Disorders : NMD|February 12, 2021
Prevalence of atrial fibrillation in myotonic dystrophy type 1: A systematic reviewVincenzo Russo, Andrea Antonio Papa, Michele Lioncino, et al.
International Journal of Toxicology|January 30, 2013
Uterotrophic assay of percutaneous lavender oil in immature female ratsValerie T Politano, Danielle McGinty, Elise M Lewis, et al.
Ophthalmology|December 9, 2009
Corneal thickness and endothelial cell characteristics in patients with myotonic dystrophyNicola Rosa, Michele Lanza, Maria Borrelli, et al.
Genes|September 28, 2023
Expanding the Natural History of <i>SNORD118</i>-Related Ribosomopathy: Hints from an Early-Diagnosed Patient with Leukoencephalopathy with Calcifications and Cysts and Overview of the LiteratureDavide Politano, Guido Catalano, Elena Pezzotti, et al.
Cancer Research|November 1, 1983
Effect of retinoic acid on the growth and morphology of a prostatic adenocarcinoma cell line cloned for the retinoid inducibility of alkaline phosphataseD H Reese, B Gordon, H G Gratzner, et al.
Neuromuscular Disorders : NMD|February 13, 2010
Early onset of cardiomyopathy and primary prevention of sudden death in X-linked Emery-Dreifuss muscular dystrophyGerardo Nigro, Vincenzo Russo, Vega Maria Ventriglia, et al.
Neuromuscular Disorders : NMD|January 17, 2012
Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying a heterozygous CAV3 T78M mutation and a D4Z4 partial deletion: Further evidence for "double trouble" overlapping syndromesGiulia Ricci, Isabella Scionti, Greta Alì, et al.
Pageof 64

Showing results (371-380 of 638) with videos related to

Sort By:
Pageof 64
The Journal of Molecular Diagnostics : JMD|December 5, 2009
One hundred twenty-one dystrophin point mutations detected from stored DNA samples by combinatorial denaturing high-performance liquid chromatographyAnnalaura Torella, Amelia Trimarco, Francesca Del Vecchio Blanco, et al.
Brain & Development|November 29, 2022
A novel variant in NEUROD2 in a patient with Rett-like phenotype points to Glu130 codon as a mutational hotspotDavide Politano, Simone Gana, Elena Pezzotti, et al.
Journal of Cardiovascular Electrophysiology|October 4, 2019
SERUM cardiac-specific biomarkers and atrial fibrillation in myotonic dystrophy type IVincenzo Russo, Anna Rago, Luigi Atripaldi, et al.
Neuromuscular Disorders : NMD|February 12, 2021
Prevalence of atrial fibrillation in myotonic dystrophy type 1: A systematic reviewVincenzo Russo, Andrea Antonio Papa, Michele Lioncino, et al.
International Journal of Toxicology|January 30, 2013
Uterotrophic assay of percutaneous lavender oil in immature female ratsValerie T Politano, Danielle McGinty, Elise M Lewis, et al.
Ophthalmology|December 9, 2009
Corneal thickness and endothelial cell characteristics in patients with myotonic dystrophyNicola Rosa, Michele Lanza, Maria Borrelli, et al.
Genes|September 28, 2023
Expanding the Natural History of <i>SNORD118</i>-Related Ribosomopathy: Hints from an Early-Diagnosed Patient with Leukoencephalopathy with Calcifications and Cysts and Overview of the LiteratureDavide Politano, Guido Catalano, Elena Pezzotti, et al.
Cancer Research|November 1, 1983
Effect of retinoic acid on the growth and morphology of a prostatic adenocarcinoma cell line cloned for the retinoid inducibility of alkaline phosphataseD H Reese, B Gordon, H G Gratzner, et al.
Neuromuscular Disorders : NMD|February 13, 2010
Early onset of cardiomyopathy and primary prevention of sudden death in X-linked Emery-Dreifuss muscular dystrophyGerardo Nigro, Vincenzo Russo, Vega Maria Ventriglia, et al.
Neuromuscular Disorders : NMD|January 17, 2012
Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying a heterozygous CAV3 T78M mutation and a D4Z4 partial deletion: Further evidence for "double trouble" overlapping syndromesGiulia Ricci, Isabella Scionti, Greta Alì, et al.
Pageof 64